Canonical Allele Identifier: CA403381045
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090671-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090671A>C , CM000681.2:g.4090671A>C GRCh38
NC_000019.9:g.4090669A>C , CM000681.1:g.4090669A>C GRCh37
NC_000019.8:g.4041669A>C NCBI36
NG_007996.1:g.38458T>G , LRG_750:g.38458T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1569T>G
ENST00000688002.1:n.3281T>G
ENST00000688751.1:n.266T>G
ENST00000689792.1:n.1034T>G
ENST00000262948.10:c.1130T>G MANE Select ENSP00000262948.4:p.Val377Gly
ENST00000262948.9:c.1130T>G ENSP00000262948.3:p.Val377Gly
ENST00000394867.8:c.839T>G ENSP00000378336.1:p.Val280Gly
ENST00000597263.5:n.315T>G
ENST00000599021.1:c.240T>G
ENST00000600584.5:n.2579T>G
ENST00000601786.5:n.1431T>G
NM_030662.3:c.1130T>G , LRG_750t1:c.1130T>G NP_109587.1:p.Val377Gly
XM_006722799.2:c.851T>G XP_006722862.1:p.Val284Gly
XM_011528133.1:c.560T>G XP_011526435.1:p.Val187Gly
NM_030662.4:c.1130T>G MANE Select NP_109587.1:p.Val377Gly